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HRID 77322作成日:2026年10月24日

Triethylamine → Trifluoromethanesulfonate

https://huagongshe.com/ja/reaction/77322

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物N-Isoamyl-N-(6-hydroxy naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 67155390—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物TrifluoromethanesulfonateHCID 2758875—
生成物N-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 86653275—

反応条件

温度0 °C

反応手順

To a solution of N-isoamyl-N-(6-hydroxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester (0.18 g, 0.35 mmol) in dichloromethane (10 mL) at 0° C. is added triethylamine (0.099 mL, 0.71 mmol), triflic anhydride (0.089 mL, 0.53 mmol), and 4-dimethylaminopyridine (0.004 g, 0.035 mmol). The reaction is stirred at 0° C. for 1 hour. The solvents are removed in vacuo, and the residue is purified by column chromatography (6% hexanes-ethyl acetate) to afford the title compound (a triflate) as a yellow solid (0.14 g, 68% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841291B2
出典データセットuspto-grants-2014_09
ORD IDord-ff2caca0eef64b8a8e81656a051c760e
出典メモuspto-grants-2014_09